Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Hazard for aquatic organisms

Freshwater

Hazard assessment conclusion:
no hazard identified

Marine water

Hazard assessment conclusion:
no hazard identified

STP

Hazard assessment conclusion:
no hazard identified

Sediment (freshwater)

Hazard assessment conclusion:
no hazard identified

Sediment (marine water)

Hazard assessment conclusion:
no hazard identified

Hazard for air

Air

Hazard assessment conclusion:
no hazard identified

Hazard for terrestrial organisms

Soil

Hazard assessment conclusion:
no hazard identified

Hazard for predators

Secondary poisoning

Hazard assessment conclusion:
no potential for bioaccumulation

Additional information

Conclusion on classification

Classification relevant information:

Water solubility: > 2054 g/L at 20 °C (EU Method A.6, flask method)

Degradation:

Biodegradation: readily biodegradable (62% degradation after 28 d, OECD 301 F)

Bioaccumulation:

 Log Kow = < -2.7 at 20 °C (EU Method A.8 - Appendix I, estimation method)

 

Aquatic acute toxicity

Fish: LC50 (96 h) > 100 mg/L (nominal, OECD 203, Danio rerio)

Aquatic invertebrates: EC50 (48 h) > 100 mg/L (nominal, OECD 202, Daphnia magna)

Algae/aquatic plant: ErC50 (72 h) > 100 mg/L (nominal, OECD 201, Pseudokirchneriella subcapitata)

 

Aquatic chronic toxicity

Algae/aquatic plant: ErC10 (72 h) > 100 mg/L (nominal, OECD 201, Pseudokirchneriella subcapitata)

Classification according to CLP

Aquatic toxicity data are available for three trophic levels (fish, aquatic invertebrates and algae). No hazard was indicated within the range of water solubility. Furthermore the substance is considered to be rapidly biodegradable. Therefore the substance does not need to be classified and labeled according to the consolidated version of Regulation (EC) No 1272/2008 and further amendments (ATPs).